# K002328: Sios-Interface for Auto Light Projector, Sios-Interface for 3 CCD Endocam, Sios-Interface for Laparo CO2 Insufflator

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Aug 27, 2001 after 391 days
- Product code: HIF (Insufflator, Laparoscopic)
- Device class: 2
- Regulation: 21 CFR 884.1730
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
22 later devices descend from it; 3 cite it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023659: 1-CCD Endocam 5520 System (2003), 10 descendants of its own
- K030082: Power Control 2303 with Power Stick M4, Model# 2303.011/.901/.911, 8564.121/.851 (2003), 8 descendants of its own
- K080977: 3 CCD Endocam 5550 (2008), 7 descendants of its own
- K130423: The Richard Wolf Endocam Logic HD Camera System 5525 (2013), 6 descendants of its own
- K041610: Morce Scope Set 8970 with Power Control 2303 and Suction Pump 2207 (2004), 6 descendants of its own

Source page: https://510kreport.com/device/K002328
Methodology: https://510kreport.com/methodology